GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Phaeobacter inhibens BS107

Align ABC transporter (characterized, see rationale)
to candidate GFF729 PGA1_c07440 ABC transporter, ATP binding protein

Query= uniprot:A0A166QFW2
         (381 letters)



>FitnessBrowser__Phaeo:GFF729
          Length = 353

 Score =  338 bits (868), Expect = 1e-97
 Identities = 189/353 (53%), Positives = 237/353 (67%), Gaps = 10/353 (2%)

Query: 1   MIKLKLDNVNKQLGGMRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICGGDL 60
           M  + L    K+ G ++++ DV L I  GEF VFVGPSGCGKSTLLR+IAGL+    G++
Sbjct: 1   MTGVTLAKAVKKYGDVQVIHDVDLSIDDGEFCVFVGPSGCGKSTLLRMIAGLEETSSGNI 60

Query: 61  LIDGRRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTDKTSLRERVLKTAQI 120
            I  R V  L+  +RGV MVFQSYALYPHM+V DN+ FGLK+    K  +RE+V + ++I
Sbjct: 61  HIGDRDVTRLDAADRGVAMVFQSYALYPHMTVEDNMGFGLKMNGHPKEKIREKVAEASRI 120

Query: 121 LQLDKLLQRKPKELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLH 180
           L+LD  L+RKPK LSGGQRQRVA+GRA+ R P++ LFDEPLSNLDA LRV MR EIARLH
Sbjct: 121 LKLDDYLKRKPKALSGGQRQRVAIGRAIVRGPEVFLFDEPLSNLDAELRVDMRVEIARLH 180

Query: 181 DRLGSTMIYVTHDQVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMN 240
             +G+TMIYVTHDQVEAMTLADKIVVL  GRVEQVGSP ELY  P +RFVAGF+GSP MN
Sbjct: 181 KEIGATMIYVTHDQVEAMTLADKIVVLRAGRVEQVGSPMELYANPDNRFVAGFIGSPSMN 240

Query: 241 FLSARLQTPGET--SLVDTLVWGITSLPFDSSNLAAGTPLSLGIRPEHVSLKAADGTAGV 298
           FL   +Q  G    +L +  V    +LP D      G+ + LG+RP+H+S+ AAD  + +
Sbjct: 241 FLEGTVQGDGVVVPALENRRVATSVALPAD------GSKVLLGLRPQHLSVTAAD--SSL 292

Query: 299 VVTAVEYLGSETYVHLETGQDEPLICRCEVSAGWQAGDRVELLLDLDNLHLFD 351
           V+   E LG  +Y +L T   E LI           G  V L  D  + ++FD
Sbjct: 293 VLDLRERLGGVSYDYLSTPTGEKLIVETRGDEALPEGTAVALGFDDADAYIFD 345


Lambda     K      H
   0.320    0.137    0.394 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 342
Number of extensions: 8
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 381
Length of database: 353
Length adjustment: 30
Effective length of query: 351
Effective length of database: 323
Effective search space:   113373
Effective search space used:   113373
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory